Interaction of intermediates with transition metal surfaces in the dehydrogenation of ethanol to ethyl acetate: A theoretical investigation. (February 2019)

• Record Type: Journal Article
• Authors: Boualouache, Adel; Boucenna, Ali; Otmanine, Ghazi
• Is Part Of: Progress in reaction kinetics and mechanism. Volume 44:Number 1(2019)
• Page Start: 74
• Page End: 91
• Publication Date: 2019-02
• Subjects: Cu-based catalyst -- transition metals -- ethanol -- ethyl acetate -- density functional theory -- unity bond index–quadratic exponential potential; Chemical kinetics -- Periodicals; 541.39405
• DOI: 10.1177/1468678319834831
• Languages: English
• ISSNs: 1468-6783

Abstract

By employing a combined approach of the unity bond index–quadratic exponential potential method and density functional theory within the generalized gradient approximation, we have studied the interaction of intermediates in the ethanol dehydrogenation process to ethyl acetate on Cu, Ag, Ni, Pd, Pt, Co, Au and Ir(111) transition metal surfaces. Binding energies and geometries were optimized for the main intermediates of this process. Electronic structures were computed for some intermediates/transition metal systems. We also calculated the activation energies for the elementary steps of the reactions. The results show that amid the studied surfaces, Cu(111) stabilizes ethoxy and acetyl species, preventing their dissociation. Inducing the η 2 binding mode of acetaldehyde by alloying Cu with Ni, Co, Pd, Pt or Ir can enhance the catalytic proprieties of the Cu(111) clean surface.